Ilaria Giordano

University Hospital Bonn — Germany

Neuroscience · Life Sciences

16h-index1.1kcitations33works0.82yr avg
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Research Topics

Genetic Neurodegenerative Diseases(31), Mitochondrial Function and Pathology(25), Neurological disorders and treatments(10), Parkinson's Disease Mechanisms and Treatments(9), Hereditary Neurological Disorders(6)

Publications33 total

Analysis of a Modified Version of the Inventory of Non‐Ataxia Signs Over 12 Years in Patients with Friedreich's Ataxia in the <scp>EFACTS</scp> Study
Movement Disorders·2025Open Access
Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias
Neurology·2025· 2 citedOpen Access
Longitudinal analysis of anthropometric measures over 5 years in patients with Friedreich ataxia in the <scp>EFACTS</scp> natural history study
European Journal of Neurology·2025· 1 citedOpen Access
Health-Related Quality of Life in Patients with Friedreich Ataxia Using Mobility Assistive Technologies: Limited Fit of the EQ-5D-3L Mobility Dimension
Neurology and Therapy·2024Open Access
Longitudinal changes of <scp>SARA</scp> scale in Friedreich ataxia: Strong influence of baseline score and age at onset
Annals of Clinical and Translational Neurology·2023· 6 citedOpen Access
Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3
Brain·2023· 11 citedOpen Access
Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult‐Onset Degenerative Ataxia
Movement Disorders·2023· 14 citedOpen Access
Prediction of the disease course in Friedreich ataxia
Scientific Reports·2022· 8 citedOpen Access
Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias
Brain Communications·2022· 33 citedOpen Access
Increased brain tissue sodium concentration in Friedreich ataxia: A multimodal MR imaging study
NeuroImage Clinical·2022· 9 citedOpen Access
Safety and Efficacy of Acetyl-DL-Leucine in Certain Types of Cerebellar Ataxia
JAMA Network Open·2021· 35 citedOpen Access
Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study
The Lancet Neurology·2021· 89 cited
Post‐haemorrhagic hydrocephalus management: Delayed neonatal transport negatively affects outcome
Acta Paediatrica·2020· 7 citedOpen Access
Onset features and time to diagnosis in Friedreich’s Ataxia
Orphanet Journal of Rare Diseases·2020· 62 citedOpen Access
Onset features and time to diagnosis in Friedreich´s Ataxia
Research Square (Research Square)·2020Open Access
Onset features and time to diagnosis in Friedreich's Ataxia
Research Square (Research Square)·2020· 3 citedOpen Access
Prominent White Matter Involvement in Multiple System Atrophy of Cerebellar Type
Movement Disorders·2020· 27 citedOpen Access
Progression Characteristics in Friedreich's Ataxia: A 4-Year Observational Study
SSRN Electronic Journal·2020Open Access
Application of Quantitative Motor Assessments in Friedreich Ataxia and Evaluation of Their Relation to Clinical Measures
The Cerebellum·2019· 12 cited
Characterization of Cerebellar Atrophy and Resting State Functional Connectivity Patterns in Sporadic Adult-Onset Ataxia of Unknown Etiology (SAOA)
The Cerebellum·2019· 7 cited
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Frequent Co-authors

Thomas Klockgether(24), Lüdger Schöls(21), Jörg B. Schulz(18), Sylvia Boesch(17), Thomas Klopstock(17), Wolfgang Nachbauer(16), Kathrin Reetz(15), Paola Giunti(15), Caterina Mariotti(14), Alexandra Dürr(14), Imis Dogan(13), Claudia Stendel(12), Massimo Pandolfo(11), Claire Didszun(11), Michael Parkinson(10), Claire Ewenczyk(10), Lorenzo Nanetti(9), Francisco Javier Rodríguez de Rivera Garrido(9), Myriam Rai(9), Dagmar Timmann(9)